A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406212



Internal ID21063765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13783411..13800097hg38UCSC Ensembl
chr6:13783643..13800329hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3816687
hg1916687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216853
Samples
Known GenesMCUR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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